V.I.E - Qualification & Validation Coordinator – Life Sciences

  • Temps complet
  • Contract Type: VIE

Description de l'entreprise

ALTEN is a world leader in Engineering and Technology Consulting with almost 60 000 employees, 88% of whom are engineers.
Operating in more than 30 countries, the Group supports its customers' development strategy in the areas of engineering, innovation, R&D and technological information systems.

Why choose ALTEN?

  • It is a great opportunity to take part in the greatest technological challenges
  • Working in a collaborative work environment provides close support
  • We are a real career booster in France and abroad

Description du poste

As a Qualification and Validation Consultant, your expertise will support the projects of our partners whose activities are established in the production of medicines or health-related products.

You will play a central role in coordinating and executing the validation cycle with the aim of successfully completing projects within the given timelines.

To do so, you will:

  • Represent the Validation department on various projects;
  • Design and implement the best Validation strategy;
  • Coordinate project planning with all stakeholders (Production / QA / Maintenance);
  • Participate in risk assessment through the drafting of a "Risk Assessment";
  • Contribute to the definition and drafting of Functional Specifications (FS) and Design Specifications (DS);
  • Write protocols, coordinate, and ensure the proper execution of tests (URS / FAT / SAT / IQ / OQ / PQ);
  • Analyze and interpret results in order to draft the corresponding reports;
  • Develop training sessions and coach operators in the field; Manage deviations related to validation runs and implement the associated CAPAs.

Qualifications

  • A degree in Engineering, a Master’s in Bioengineering, Industrial Pharmacy, or related fields;
  • Experience in qualification and validation within a GMP environment;
  • Knowledge of production processes in the pharmaceutical industry;
  • The ability to work in English as well as French.
  • Curious to learn more about production equipment and/or manufacturing processes;
  • Organized and meticulous in drafting your GMP documentation;
  • Communicative and enjoy interacting with various departments such as Production / Quality Assurance / Maintenance.